Canonical Allele Identifier: CA1047033615

Gene: SCN11A

Linked Data

• dbSNP Id: rs2031788596
• gnomAD v3: 3-39032588-AG-A
• gnomAD v4: 3-39032588-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39032589del , CM000665.2:g.39032589del	GRCh38
NC_000003.11:g.39074080del , CM000665.1:g.39074080del	GRCh37
NC_000003.10:g.39049084del	NCBI36
NG_033859.2:g.24398del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302328.9:c.-403-86del MANE Select	ENSP00000307599.3:n.-403-86del
ENST00000665106.1:n.82-86del
ENST00000668754.1:c.-903-86del	ENSP00000499569.1:n.-903-86del
ENST00000674755.1:n.233-86del
ENST00000675269.1:n.125-86del
ENST00000676333.1:n.39-86del
XM_011534335.1:c.49-86del	XP_011532637.1:n.49-86del
XM_011534336.1:c.49-86del	XP_011532638.1:n.49-86del
XR_940736.1:n.79-86del
XR_940737.1:n.79-86del
XR_940738.1:n.79-86del
XR_940739.1:n.79-86del
NM_001349253.1:c.-403-86del	NP_001336182.1:n.-403-86del
NM_001349253.2:c.-403-86del MANE Select	NP_001336182.1:n.-403-86del
NR_164473.1:n.85-86del